{"title":"Sustainable lactic acid production from glycerol via hydrothermal catalysis over highly dispersed cu nanoparticles on bio-tar derived carbon","authors":"Han Xu , Qi Li , Zhihao Bi, Donghai Xu, Yang Guo","doi":"10.1016/j.jece.2025.119275","DOIUrl":null,"url":null,"abstract":"<div><div>Copper-based catalysts have emerged as promising candidates for the catalytic conversion of glycerol to lactic acid (LA), owing to their cost-effectiveness and high activity. However, optimizing both high conversion efficiency and selectivity in catalytic design remains a significant challenge in the catalytic design for this synthesis. In this study, we developed a highly efficient Cu-based catalyst (Cu/BC) was by optimizing copper loading on biomass tar-derived porous carbon supports. Through systematic investigation of reaction parameters and copper loading effects, the results revealed that the 20 % Cu/BC catalyst achieved exceptional performance, achieving 98.97 % glycerol conversion and 89.88 % LA selectivity under optimized conditions (210°C, 20 h). This superior activity stems from the highly dispersed metallic copper active sites, which enhances reaction kinetics and product selectivity. Notably, excessive copper loading (>20 %) induced metal aggregation, pore blockage, and diffusion limitations, thereby diminishing catalytic performance and promoted side reactions. Kinetic analysis further revealed that the 20 % Cu/BC catalyst exhibited a lower activation energy (110.5 kJ·mol<sup>−1</sup>) compared to the 25 % Cu/BC counterpart (125.8 kJ·mol<sup>−1</sup>) in the disappearance of LA, confirming its superior catalytic efficiency. This work not only advances rational design of non-noble metal catalysts but also provides a sustainable strategy for value-added LA production.</div></div>","PeriodicalId":15759,"journal":{"name":"Journal of Environmental Chemical Engineering","volume":"13 6","pages":"Article 119275"},"PeriodicalIF":7.2000,"publicationDate":"2025-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Environmental Chemical Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2213343725039715","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Copper-based catalysts have emerged as promising candidates for the catalytic conversion of glycerol to lactic acid (LA), owing to their cost-effectiveness and high activity. However, optimizing both high conversion efficiency and selectivity in catalytic design remains a significant challenge in the catalytic design for this synthesis. In this study, we developed a highly efficient Cu-based catalyst (Cu/BC) was by optimizing copper loading on biomass tar-derived porous carbon supports. Through systematic investigation of reaction parameters and copper loading effects, the results revealed that the 20 % Cu/BC catalyst achieved exceptional performance, achieving 98.97 % glycerol conversion and 89.88 % LA selectivity under optimized conditions (210°C, 20 h). This superior activity stems from the highly dispersed metallic copper active sites, which enhances reaction kinetics and product selectivity. Notably, excessive copper loading (>20 %) induced metal aggregation, pore blockage, and diffusion limitations, thereby diminishing catalytic performance and promoted side reactions. Kinetic analysis further revealed that the 20 % Cu/BC catalyst exhibited a lower activation energy (110.5 kJ·mol−1) compared to the 25 % Cu/BC counterpart (125.8 kJ·mol−1) in the disappearance of LA, confirming its superior catalytic efficiency. This work not only advances rational design of non-noble metal catalysts but also provides a sustainable strategy for value-added LA production.
期刊介绍:
The Journal of Environmental Chemical Engineering (JECE) serves as a platform for the dissemination of original and innovative research focusing on the advancement of environmentally-friendly, sustainable technologies. JECE emphasizes the transition towards a carbon-neutral circular economy and a self-sufficient bio-based economy. Topics covered include soil, water, wastewater, and air decontamination; pollution monitoring, prevention, and control; advanced analytics, sensors, impact and risk assessment methodologies in environmental chemical engineering; resource recovery (water, nutrients, materials, energy); industrial ecology; valorization of waste streams; waste management (including e-waste); climate-water-energy-food nexus; novel materials for environmental, chemical, and energy applications; sustainability and environmental safety; water digitalization, water data science, and machine learning; process integration and intensification; recent developments in green chemistry for synthesis, catalysis, and energy; and original research on contaminants of emerging concern, persistent chemicals, and priority substances, including microplastics, nanoplastics, nanomaterials, micropollutants, antimicrobial resistance genes, and emerging pathogens (viruses, bacteria, parasites) of environmental significance.